EP4010514A1

EP4010514A1 - Electrolyser device and method for carbon dioxide reduction

Info

Publication number: EP4010514A1
Application number: EP20797406.4A
Authority: EP
Inventors: David Reinisch; Nemanja Martic; Günter Schmid
Original assignee: Siemens Energy Global GmbH and Co KG
Current assignee: Siemens Energy Global GmbH and Co KG
Priority date: 2019-10-25
Filing date: 2020-10-16
Publication date: 2022-06-15
Also published as: AU2020369070B2; WO2021078635A1; AU2020369070A1; CN114585773A

Abstract

The invention relates to an electrolyser for carbon dioxide reduction, comprising an electrolytic cell (4), with a cathode gas diffusion electrode (6) and an anode gas diffusion electrode (8), in which a first side (12) of the cathode gas diffusion electrode (8) adjoins a cathode gas chamber (10) in a planar manner and likewise a first side (13) of the anode gas diffusion electrode (8) adjoins an anode gas chamber (14), and an electrolyte chamber (16) common to both gas diffusion electrodes (6, 8) is provided, which extends from the cathode gas diffusion electrode (6) to the anode gas diffusion electrode (8) and is at least partially delimited by the two gas diffusion electrodes (6, 8) with their second sides (18, 19) facing away from the respectively associated gas chambers (10, 14).

Description

description

Electrolyser and process for carbon dioxide reduction

The invention relates to an electrolyzer for carbon dioxide reduction. Carbon dioxide is transported past a gas diffusion cathode of an electrolysis cell and there catalytically reduced to at least one energetically higher-value product.

Introduction and state of the art

Burning fossil fuels currently covers around 80% of the world's energy needs. In 2011, around 34,032.7 million tons of carbon dioxide were emitted into the atmosphere as a result. This release of carbon dioxide is the easiest way to dispose of large amounts of carbon dioxide. In lignite power plants, for example, over 50,000 tons are produced every day. However, the discussion about the negative effects of the greenhouse gas carbon dioxide on the climate has led to the fact that recycling of carbon dioxide is desirable and that work is being done on this. Since, from a thermodynamic point of view, carbon dioxide is very low, it is difficult to reduce it to useful products.

The carbon dioxide is converted naturally into carbohydrates through photosynthesis. This process, which is broken down into many sub-steps in terms of time and space at the molecular level, is very difficult to copy on an industrial scale. Compared to pure photocatalysis, the electrochemical reduction of carbon dioxide is currently the most efficient way. A hybrid form is light-assisted electrolysis or electrically assisted photo-catalysis. Both terms are to be used synonymously, depending on the perspective of the observer. As with photosynthesis, in this process, with the addition of electrical energy, if necessary photo-assisted, which is preferably obtained from regenerative energy sources such as wind or sun, carbon dioxide is converted into an energetically higher-value product such as carbon monoxide, methane, ethene or other alcohols. The amount of energy required for this reduction ideally corresponds to the combustion energy of the fuel and should only come from regenerative sources.

Some possible ways of producing energy sources and chemical raw materials based on renewable energies are currently being discussed. Particularly desirable is the direct electrochemical or photochemical conversion of carbon dioxide into hydrocarbons or their oxygen derivatives. There are currently no industrial catalysts available for these direct routes. Therefore, multi-stage routes are being discussed which, due to the higher level of technical maturity of the individual steps, promise a timely solution. The most important intermediate in these multi-level value chains is carbon monoxide. It is commonly regarded as the most important Cl building block in synthetic chemistry. As a synthesis gas mixture, i.e. hydrogen and carbon monoxide in a ratio greater than 2: 1, it can be used via the Fischertropsch process to build up hydrocarbons and to synthesize methanol. Gas mixtures richer in carbon monoxide or pure carbon monoxide are also used for carbonylation reactions such as hydroformulation by carboxylic acid synthesis or alcohol carbonylation, in which the primary carbon chain is lengthened. The possibility of generating carbon monoxide from carbon dioxide with the inclusion of regenerative energy sources opens up a multitude of possibilities for partially or fully replacing fossil raw materials as a source of carbon for many chemical products. One of these routes is the electrochemical breakdown of carbon dioxide into carbon monoxide and oxygen. This is a one-step process that does not require high temperatures or overpressure. However, it is a relatively complex electrolysis process in which carbon dioxide has to be added as a substrate as a gaseous substrate. In addition, the gaseous carbon dioxide can react with the charge carriers generated in the electrolysis and is therefore chemically bound in the electrolyte used:

During the process, these carbonates are then broken down again as a result of the proton generation at the anode:

Depending on the educt composition and in particular influenced by different catalyst materials in the gas diffusion electrodes, other reactions can also take place while maintaining the reduction of the CO 2.

Depending on the structure of the electrolytic cell, the release takes place either in the electrolyte, on a membrane contact surface or directly on the anode. In the first two cases, gas bubbles are released in the ionic current path, which can lead to greatly increased cell voltages and thus to massive losses in energy efficiency. In the latter case, a mixture of carbon dioxide and oxygen would be formed at the anode. There are currently no possible uses for such mixtures and separation would be necessary, but very costly. Classic carbon dioxide separation processes such as amine or methanol washes cannot be used for safety reasons. For such electrochemical cells for the decomposition of carbon dioxide into carbon monoxide and oxygen, purified carbon dioxide is also used. Accordingly, it represents a significant loss of resources when carbon dioxide is lost through a gas mixture of oxygen and carbon dioxide generated at the anode. This loss of resources significantly increases operating costs. In addition, with the predominant release of carbon dioxide, the technology loses its character as a green technology. Recirculation of the entire gas into the feed gas stream is inefficient, since the electrochemically generated oxygen in the feed gas stream would be reduced back to water and thus the efficiency of the electrolysis system and process would be reduced.

From DE 102018 210 303 A1 a method for the electrochemical conversion of a gas comprising CO2 and a device for the electrochemical conversion of a gas comprising CO2 are known, a gas comprising H2 being converted at an anode of an electrolysis cell.

DE 102018 202 184 A1 discloses an electrolysis cell comprising a cathode space comprising a cathode, an anode space comprising an anode, and a salt bridge space which is arranged between the cathode and anode, the cathode and the anode being designed as a gas diffusion electrode.

In US 2012/0228 147 A1, methods and devices for the electrochemical production of formic acid are described ben.

There is therefore a need for a carbon dioxide electrolyzer by means of which an electrochemical breakdown of carbon dioxide into carbon monoxide and oxygen can take place, in which at the same time the carbon dioxide losses via the gas mixture formed at the anode are minimized and carbon dioxide entries into the electrolyte are separated as completely as possible can be. The object is achieved in an electrolyzer with the features of claim 1 and in a method with the features according to claim 12.

The electrolyser according to the invention according to claim 1 for carbon dioxide reduction comprises an electrolysis cell with a cathode gas diffusion electrode and with an anode gas diffusion electrode. The cathode gas diffusion electrode (hereinafter also abbreviated as GDK) adjoins a cathode gas space on a flat first side. The first side of the anode gas diffusion electrode (GDA) also adjoins an anode gas space over a large area. The two gas diffusion electrodes each have a second side which is opposite the respective first side and which is connected to a common electrolyte space. The electrolyte space is designed in such a way that it extends from the cathode gas diffusion electrode to the anode gas diffusion electrode and is at least partially delimited by the two gas diffusion electrodes with their second side facing away from the respectively assigned gas spaces. The anode gas diffusion electrode has a cation-selective coating.

The electrolysis cell of the electrolyzer according to claim 1 has two gas diffusion electrodes, namely a gas diffusion electrode on the anode (GDA) and one on the cathode (GDK). Both gas diffusion electrodes are connected to their own separate gas space, and they each delimit this separate gas space from a common electrolyte space. The described electrolytic cell of the electrolyzer thus has only one electrolyte space, which is not separated by a membrane or a diaphragm. The electrolyte located in the electrolyte space and flowing through it is thus connected to both gas diffusion electrodes.

It has been found experimentally that the structure of an electrolyser with these two essential features, namely two gas diffusion electrodes both on the anode and on the cathode and a common, not separate electrolyte space, means that carbon dioxide that gets through the GDK into the electrolyte space can dissolve in this in an oversaturated manner and be discharged from the electrolyte space before it mixes with the oxygen produced there at the GDA and thus becomes economically unusable for the further process feed. As described, the oxygen is created at the GDA, which diffuses through it and is discharged through the separate gas space of the GDA. Mixing of the generated oxygen with the carbon dioxide is thus greatly reduced. The reduction can be reduced to 5% of the value that is usual in a conventional design with a gas diffusion electrode and two separate electrolyte chambers.

In one embodiment of the invention, the electrolyte space is provided with an electrolyte supply line and an electrolyte discharge line, which together with a pumping device form an electrolyte circuit. It is therefore also a common electrolyte circuit for the entire electrolyzer, which makes two separate electrolyte reservoirs or a neutralization of the respective reservoirs superfluous.

Furthermore, a cathode gas space and an educt gas supply device for supplying educt gases are expediently provided.

Furthermore, it is expedient to install a carbon dioxide separation device in the electrolyte circuit, as a result of which the carbon dioxide in the electrolyte can be discharged and can be fed back to the educt gas through a corresponding further advantageous connecting line.

Furthermore, in an advantageous embodiment, the anode compartment has an oxygen discharge device. Through this Oxygen that has entered the anode gas space through the anode can be extracted from the process.

According to the invention it is provided that the GDA is designed in such a way that it has a cation-selective coating.

In this case, the GDA is coated with an ion-conducting polymer. This can conduct the protons produced into the electrolyte, but is impermeable to gases. Therefore, CO2 gas bubbles cannot enter the anode gas space and molecular gaseous oxygen that forms on the anode cannot get into the electrolyte. The cation-selective coating is preferably located on a side which is directed towards the electrolyte space, as a result of which an effective transport of protons into the electrolyte can be achieved.

Another component of the invention is a method for operating an electrolyzer having the features of patent claim 8. This method comprises the following steps: introducing a carbon dioxide-containing gas into a cathode gas space. In this case, the carbon dioxide is reduced to carbon monoxide on a cathode gas diffusion electrode, the cathode gas diffusion electrode resting on a first side against the cathode gas space and with the opposite, second side resting against an electrolyte space. The cathode gas diffusion electrode is flat and has the first and second flat sides, with one side resting against the cathode gas space and the other side resting against the electrolyte space.

A liquid electrolyte flows through the electrolyte space, in which carbon dioxide is in turn dissolved.

Furthermore, molecular oxygen is released on an anode gas diffusion electrode surface, which oxygen diffuses through an anode gas diffusion electrode. Both the cathode gas diffusion electrode and the anode gas diffusion electrode adjoin the common electrolyte space with the second side in each case.

In addition, the electrolyte outside the electrolyte space is discharged from the CO2 dissolved in it.

The anode gas diffusion electrode has a cation-selective coating in the process. In particular, the method according to the invention is carried out with the electrolyzer according to the invention. Embodiments that have been described with respect to the electrolyser can be used accordingly in the method according to the invention, and vice versa.

As already mentioned with regard to claim 1, the claimed method also has the special feature that the electrolyte space is a common electrolyte space for both the cathode and the anode and therefore has no corresponding separation such as a membrane or diaphragm. Furthermore, both the anode and the cathode are each designed as a gas diffusion electrode, GDA and GDK. This has the effect that oxygen, which is released in the electrolyte during the process, can diffuse through the anode gas diffusion electrode as molecular oxygen and does not mix with the carbon dioxide that is also formed in the electrolyte. This in turn has the consequence that the carbon dioxide in the electrolyte can be in supersaturated form and can be led out of the electrolyte compartment and can be discharged from the electrolyte outside the electrolyte compartment. This discharged carbon dioxide can be fed back into the process as educt gas, which makes the overall process significantly more economical.

In the method described, it is expedient that the pH value of the electrolyte is in the acidic range, with a slightly acidic range between a pH value between 7 and 2 is aimed at. The electrolyte is in particular an aqueous electrolyte.

Furthermore, it is expedient that a gas volume flow of the carbon dioxide at the gas diffusion cathode is at least 5 times as large, in particular 15 times as large, as at the gas diffusion anode. This leads to a further increase in the economic efficiency of the process.

Further embodiments and further examples and features of the invention are explained in more detail in the context of the following description of the figures. These are purely exemplary embodiments that do not represent any restriction of the scope of protection.

Show:

Figure 1 shows an electrolyzer with a schematic representation of the individual process devices,

FIG. 2 shows a very schematic representation of the material flow in the electrolyser according to FIG. 1 with the representation of the individual chemical components

Figure 3 shows a cross section through an anode gas diffusion electrode and

FIG. 4 is a diagram showing the gas volume flow in different areas in the electrolyzer.

The electrolyser 2 according to FIG. 1 is shown there in a very schematic manner with regard to its structure. The electrolyser 2 comprises an electrolysis cell 4 in which, in turn, two gas diffusion electrodes are arranged. This is a cathode gas diffusion electrode 6 (hereinafter referred to as GDK). Furthermore, an anode gas diffusion electrode 8 is provided, which is referred to below as GDA. Both gas diffu- Sion electrodes 6, 8 are designed as flat structures which each have two flat sides and thereby separate a gas space from an electrolyte space 16. In detail, this is structured as follows:

The GDK 6 has a first side 12 which is connected to a cathode gas space 10 or at least partially delimits it from the electrolyte space 16. The electrolyte space 16 is in turn connected to a second side 18 of the GDK 6. Furthermore, the GDA 8 likewise has a second side 19 which delimits the electrolyte space 16 from the other side. The first side of the GDA 13 in turn adjoins a further gas space, namely the anode gas space 14. The two gas diffusion electrodes 6, 8 thus at least partially delimit the electrolyte space 16 from two sides. What is special about the structure described is that, in contrast to other electrolyser structures or electrolysis cells according to the prior art, the electrolyte space 16 has no separation between the two electrodes. There is only one common electrolyte space 16 between the GDK 6 and the GDA 8. There is no continuous structure such as a membrane or a diaphragm. A liquid electrolyte 42, which is located in the electrolyte space 16 in the operating state, is in direct connection both with the second side 18 of the GDK 6 and with the second side 19 of the GDA 8.

The electrolysis cell 42 described thus has essential features. On the one hand, instead of the usual one gas diffusion electrode as the cathode, two gas diffusion electrodes are used in the case described, in this case the anode configured as GDA 8 is thus also a gas diffusion electrode. Furthermore, there is only one common electrolyte space for both electrodes. The mode of action of this structure will be discussed later.

First of all, it should be explained with regard to FIG. 1 that an electrolyte circuit 26 is provided which has both an rolyte feed line 20 as well as an electrolyte discharge line 22 and a pumping device 24. Furthermore, a CCh separation device 32 is provided in the electrolyte circuit 26, which in turn leads via a connecting line 34, possibly via a CO 2 processing device 46, to an educt gas supply device 28. Furthermore, an electrolyte reservoir 44 is provided in the electrolyte circuit 26.

For the supply of the electrolysis cell 4 or the electrolyzer 2 with educts and the removal of products, the educt feed device 28 is provided, as already mentioned, in which an educt gas 40, which comprises carbon dioxide, is introduced into the cathode gas space 10. The cathode gas space 10 also includes a product gas outlet device 30, in which the carbon monoxide and excess carbon dioxide formed during the process are discharged. The electrolysis cell also includes the anode gas space 14, which has an oxygen discharge device 36. The voltage U is applied between the two gas diffusion electrodes 6 and 8. In an embodiment according to the invention, the anode gas diffusion electrode has a cation-selective coating (not shown).

In FIG. 2, the electrolyzer 2 described with reference to FIG. 1 is shown once again more schematically, the purpose of which is to illustrate the course of the reaction and the substance flow using the chemical symbols. In this case, essentially carbon dioxide is introduced into the cathode gas space 10 as the starting gas and at least partially reduced to carbon monoxide on the first surface 12 of the GDK and discharged again through the product gas outlet device 30 described. Since most of the processes do not lead to a complete reduction of the total carbon dioxide (CO2) to carbon monoxide (CO), both carbon dioxide and carbon monoxide are discharged in the outlet device 30 and are later separated from one another. As shown by the chemical equations Eq. 1 to Eq. 4 is described, the Koh lendioxid also passes through the GDK 6 in the electrolyte space 16, where it reacts with the water present there to form hydrocarbonate anions (cf. equation 1 and equation 2).

In contrast, both protons and molecular oxygen are produced at the GDA (cf. equation 3), with the protons reacting with the carbonate ions to form carbon dioxide and water (equation 4).

The carbon dioxide recovered in this way is dissolved in the electrolyte 42, possibly strongly supersaturated, and discharged with this from the electrolyte cell 2 or the electrolyte chamber 16. The discharged carbon dioxide can be removed again from the electrolyte 42 in the electrolyte circuit 26 in the described C0 ₂ separation device 32 and fed back to the educt gas 40. In this case, the carbon dioxide can optionally also be processed in a processing device 46.

As can already be seen in equation 3, molecular oxygen ( _{O 2) is} generated at the GDA 8, which can diffuse through the GDA 8 and thus get into the anode gas space 14 and escape via the oxygen discharge device 36. Only by designing the anodes in the form of a GDA 8 is it possible that the molecular oxygen that is inevitably generated in the process does not mix with the carbon dioxide in the electrolyte and then has to be separated from it again later. As shown in FIG. 3, the GDA 8 is provided with a hydrophobic layer 38 so that the molecular oxygen can diffuse through the GDA 8, but the liquid water is retained by the aforementioned hydrophobic layer 38. As described, the carbon dioxide is dissolved in a relatively pure form in the electrolyte 42 and can be removed therefrom and fed back into the process. A complex separation of a carbon dioxide-oxygen mixture is not necessary, which is why the process is made much more efficient.

In a conventional process management, it is assumed that about half of the carbon dioxide introduced is lost through the process, in particular through the mixture with molecular oxygen, at least economically during the process. Economically lost is understood to mean that it is not profitable to separate the already contaminated carbon dioxide from the oxygen again under economic standards.

To illustrate this, the gas volume flows 50 of the gases essentially involved in the process (O2, CO, CO2 and H2) at the individual electrodes or in the electrolyte are shown in FIG. The individual gas volume flows 50 can be recognized by means of different hatching. The gas volume flow 51 of the carbon dioxide is of particular interest here. As on the left bar, which illustrates the gas volume flow 52 at the GDK 6, there is a very high carbon dioxide content here, but the essential carbon monoxide content is also present at this point, i.e. at the GDK. The gas volume flow 54 in the electrolyte 42 (middle bar) also shows a high carbon dioxide gas volume flow, there is only very little carbon monoxide included. This shows that the electrolyte almost only absorbs carbon dioxide as a gas, as already described, in saturated form, which is separated again from the electrolyte 42 in the further course of the process. The gas volume flow 56 at the GDA 8 has only a very small proportion of the gas volume flow 51 of the carbon dioxide. With good process management, this can only amount to only a 20th of the gas volume flow 51 at the GDK 6. This means that via the GDA 8, only a 20th of the carbon dioxide used together with the Oxygen is diverted and thus lost. As already explained, this value is up to 50% of the carbon dioxide used in conventional processes.

FIG. 4 thus illustrates that the measures taken in the CCh electrolyzer 2 presented here, namely the use of two gas diffusion electrodes as GDK 6 and GDA 8 and an electrolyte space 16 enclosed by them, leads to the loss of carbon dioxide oxide can be reduced from approx. 50% to approx. 5% or even less during electrolysis. Ultimately this means a reduction in carbon dioxide loss of more than 90%.

The GDA 8 has a hydrophobic layer 38 which prevents penetration of the electrolyte 42, which is in particular water-based. However, the molecular oxygen can diffuse through the pores of the GDA 8 into the anode gas space 14.

Since CO2 can also be present in a highly supersaturated concentration in aqueous solution, the CO2 present as a result of the neutralization (equation 4) does not necessarily have to lead to the formation of gas bubbles in the electrolyte space 16. In particular, due to the low concentrations of anodically formed H ⁺ and cathodically formed carbonates, the neutralization is distributed over the entire electrolyte space 16. Due to the possible oversaturation, the outgassing is distributed over the entire electrolyte 42 in the electrolyte space 16 and the electrolyte circuit 26, which also includes the electrolyte reservoir 44. The CO2 bubbles present in the electrolyte 42 can be separated from the electrolyte 42 before entering the electrolysis cell. This takes place in the described C0 ₂ separation device 32. This distributes the release of the carbon dioxide chemically bound by the cathode reaction and only a small part of the gas bubbles is actually released in the electrolyte space 16. There are three options for the carbon dioxide bubbles released in the electrolyte compartment 16:

You come into contact with the GDK 6 and are absorbed by it. In this case, the carbon dioxide is made available again for the reaction. This case is advantageous for the process flow.

The CO2 bubbles come into contact with the GDA and are absorbed by it. In this case, the carbon dioxide dissolved by the reaction mixes with the anodically formed oxygen in the anode gas space 14. This part corresponds to the gas volume flow 51 of the carbon dioxide in the right bar 56 of FIG. 4. This carbon dioxide can be regarded as lost for the process.

In the third possible case, the _{CO 2} gas bubbles do not come into contact with either of the two gas diffusion electrodes 6, 8 and are carried out of the electrolysis cell 4 with the electrolyte 42. This part of the carbon dioxide can be separated from the liquid electrolyte 42 with the remaining electrolyte 42 as described and, after any processing (CCb processing device 46), can be made available again to the gas cycle, in particular to the educt gas 40, via the connecting line 34.

List of reference symbols

2 electrolyzer

4 electrolytic cell

6 cathode gas diffusion electrode (GDK)

8 anode gas diffusion electrode (GDA)

10 cathode gas compartment

12 first page GDK

13 first page GDA

14 anode gas compartment

16 electrolyte room

18 second page GDK

19 second page GDA

20 Electrolyte supply line

22 Electrolyte drainage

24 pumping device

26 Electrolyte circuit

28 Feed gas feed

30 Product gas outlet device

32 CCb separator

34 connecting cable

36 Oxygen deflation device

38 hydrophobic coating

40 feed gas

42 electrolyte

44 electrolyte reservoir

46 CCb preparation

48 product gas

50 gas volume flow

51 Gas volume flow CO2

52 Gas volume flow GDK

54 Gas volume flow electrolyte

56 Gas volume flow GDA

Claims

1. Electrolyser for carbon dioxide reduction, comprising an electrolysis cell (4), with a cathode gas diffusion electrode (6) and with an anode gas diffusion electrode (8), the cathode gas diffusion electrode (8) on a first side (12) flat against a cathode gas space (10) adjoins and the anode gas diffusion electrode (8) also adjoins an anode gas space (14) with a first side (13), and an electrolyte space (16) common to both gas diffusion electrodes (6, 8) is provided, which is connected to the cathode gas diffusion electrode (6 ) extends to the anode gas diffusion electrode (8) and is delimited at least in sections by the two gas diffusion electrodes (6, 8) with their second side (18, 19) facing away from the respectively assigned gas spaces (10, 14), the anode gas diffusion electrode (8) has a cation-selective coating.

2. Electrolyzer according to claim 1, characterized in that the electrolyte space (16) is provided with an electrolyte feed device (20) and an electrolyte discharge line (22) which together with a pump device (24) form an electrolyte circuit (26).

3. Electrolyser according to one of claims 1 or 2, characterized in that the cathode gas space (10) has an educt gas supply device (28) and a product gas outlet device (30).

4. Electrolyser according to claim 2 or 3, characterized in that a CO2 separator (32) is provided in the electrolyte circuit (26).

5. Electrolyser according to claim 4, characterized in that there is a connecting line (34) from the CCb separator (32) to the educt gas supply device (28). 6. Electrolyser according to one of the preceding claims, characterized in that an oxygen discharge device (36) is provided on the anode gas space (14).

7. Method for operating an electrolyzer (2), comprising the following steps:

- Introducing a CC ^ -containing educt gas (40) into a cathode gas space (10),

- wherein the CO2 on a cathode gas diffusion electrode (6) is at least partially reduced to CO and the cathode gas diffusion electrode (6) with a first side (12) on the cathode gas space (10) and with the opposite second side (18) on an electrolyte space (16) ) is present,

- The electrolyte space (16) is traversed by a liquid electrolyte (42),

- CO2 is dissolved in the electrolyte (42) and

- Molecular oxygen 02 is released on an anode gas diffusion electrode surface, which diffuses through an anode gas diffusion electrode (8), wherein

- Both the cathode gas diffusion electrode (6) and the anode gas diffusion electrode (8) each with a second side (18, 19) on the common electrolyte space

(16) adjoin and

- The electrolyte (42) outside the electrolyte space (16) is discharged from the CO2 dissolved therein, the anode gas diffusion electrode (8) having a cation-selective coating.

8. The method according to claim 7, characterized in that the electrolyte (42) comprises an aqueous salt solution, where in the dissolved salt is not based on a salt of carbonic acid.

9. The method according to claim 7 or 8, characterized in that the pH value of the electrolyte (42) is less than 7. 10. The method according to claim 9, characterized in that the pH of the electrolyte (42) is between 2 and 7.

11. The method according to any one of claims 7 to 10, characterized in that the discharged from the electrolyte (42)

CO2 is fed to the CC> 2-containing feed gas (40).

12. The method according to any one of claims 7 to 11, characterized in that a gas volume flow of the CO2 at the gas diffusion cathode (6) is at least 5 times as large as at the gas diffusion anode (8).

13. The method according to claim 12, characterized in that a gas volume flow of the CO2 on the gas diffusion cathode (6) is at least 15 times as large as on the gas diffusion on anode (8).